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Showing results (51-60 of 151) with videos related to

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Neuromuscular Disorders : NMD|October 16, 2012
Presymptomatic late-onset Pompe disease identified by the dried blood spot testMatias Wagner, Amina Chaouch, Juliane S Müller, et al.
Human Molecular Genetics|March 13, 2008
Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscleYanchao Huang, Antoine de Morrée, Alexandra van Remoortere, et al.
Neurology. Clinical Practice|November 29, 2021
Preventing Cardiomyopathy in DMD: A Randomized Placebo-Controlled Drug TrialJohn P Bourke, Gillian Watson, Stefan Spinty, et al.
Human Molecular Genetics|December 2, 2005
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3Delia J Hernández-Deviez, Sally Martin, Steven H Laval, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 2009
New aspects on patients affected by dysferlin deficient muscular dystrophyLars Klinge, Ahmed Aboumousa, Michelle Eagle, et al.
Neuromuscular Disorders : NMD|March 29, 2005
Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathyEugenio Mercuri, Anne Lampe, Joanna Allsop, et al.
European Journal of Heart Failure|April 12, 2013
Subepicardial dysfunction leads to global left ventricular systolic impairment in patients with limb girdle muscular dystrophy 2IKieren G Hollingsworth, Tracey A Willis, Matthew G D Bates, et al.
Prenatal Diagnosis|July 2, 2004
Prenatal diagnosis of Ullrich congenital muscular dystrophy using haplotype analysis and collagen VI immunocytochemistryMartin Brockington, Susan C Brown, Anne Lampe, et al.
Human Molecular Genetics|March 17, 2009
Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophyYen-Hui Chiu, Mark A Hornsey, Lars Klinge, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
Pageof 16

Showing results (51-60 of 151) with videos related to

Sort By:
Pageof 16
Neuromuscular Disorders : NMD|October 16, 2012
Presymptomatic late-onset Pompe disease identified by the dried blood spot testMatias Wagner, Amina Chaouch, Juliane S Müller, et al.
Human Molecular Genetics|March 13, 2008
Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscleYanchao Huang, Antoine de Morrée, Alexandra van Remoortere, et al.
Neurology. Clinical Practice|November 29, 2021
Preventing Cardiomyopathy in DMD: A Randomized Placebo-Controlled Drug TrialJohn P Bourke, Gillian Watson, Stefan Spinty, et al.
Human Molecular Genetics|December 2, 2005
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3Delia J Hernández-Deviez, Sally Martin, Steven H Laval, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 2009
New aspects on patients affected by dysferlin deficient muscular dystrophyLars Klinge, Ahmed Aboumousa, Michelle Eagle, et al.
Neuromuscular Disorders : NMD|March 29, 2005
Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathyEugenio Mercuri, Anne Lampe, Joanna Allsop, et al.
European Journal of Heart Failure|April 12, 2013
Subepicardial dysfunction leads to global left ventricular systolic impairment in patients with limb girdle muscular dystrophy 2IKieren G Hollingsworth, Tracey A Willis, Matthew G D Bates, et al.
Prenatal Diagnosis|July 2, 2004
Prenatal diagnosis of Ullrich congenital muscular dystrophy using haplotype analysis and collagen VI immunocytochemistryMartin Brockington, Susan C Brown, Anne Lampe, et al.
Human Molecular Genetics|March 17, 2009
Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophyYen-Hui Chiu, Mark A Hornsey, Lars Klinge, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
Pageof 16